rs587783434

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs587783434(G;T)

Make rs587783434(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

60821907

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs587783434
dbSNP (classic)	rs587783434
ClinGen	rs587783434
ebi	rs587783434
HLI	rs587783434
Exac	rs587783434
Gnomad	rs587783434
Varsome	rs587783434
LitVar	rs587783434
Map	rs587783434
PheGenI	rs587783434
Biobank	rs587783434
1000 genomes	rs587783434
hgdp	rs587783434
ensembl	rs587783434
geneview	rs587783434
scholar	rs587783434
google	rs587783434
pharmgkb	rs587783434
gwascentral	rs587783434
openSNP	rs587783434
23andMe	rs587783434
SNPshot	rs587783434
SNPdbe	rs587783434
MSV3d	rs587783434
GWAS Ctlg	rs587783434

Max Magnitude

0

ClinVar
Risk	rs587783434(T;T)
Alt	rs587783434(T;T)
Reference	Rs587783434(G;G)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61734466G>T
CLNSRC
CLNACC	RCV000145660.1,